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LincRNA-p21 Impacts Prognosis in Resected Non-Small Cell Lung Cancer Patients through Angiogenesis Regulation.
Castellano, Joan J; Navarro, Alfons; Viñolas, Nuria; Marrades, Ramon M; Moises, Jorge; Cordeiro, Anna; Saco, Adela; Muñoz, Carmen; Fuster, Dolors; Molins, Laureano; Ramirez, Josep; Monzo, Mariano.
Afiliação
  • Castellano JJ; Molecular Oncology and Embryology Laboratory, Human Anatomy Unit, School of Medicine, University of Barcelona, IDIBAPS, Barcelona, Spain.
  • Navarro A; Molecular Oncology and Embryology Laboratory, Human Anatomy Unit, School of Medicine, University of Barcelona, IDIBAPS, Barcelona, Spain. Electronic address: anavarroponz@ub.edu.
  • Viñolas N; Department of Medical Oncology, Clinic Institute of Haematological and Oncological Diseases, Hospital Clinic of Barcelona, University of Barcelona, IDIBAPS (August Pi i Sunyer Biomedical Research Institute), Barcelona, Spain.
  • Marrades RM; Department of Pneumology, Thorax Clínic Institute, Hospital Clinic of Barcelona, University of Barcelona, IDIBAPS (August Pi i Sunyer Biomedical Research Institute), CIBER of Respiratory Diseases (CIBERES), Barcelona, Spain.
  • Moises J; Department of Pneumology, Thorax Clínic Institute, Hospital Clinic of Barcelona, University of Barcelona, IDIBAPS (August Pi i Sunyer Biomedical Research Institute), CIBER of Respiratory Diseases (CIBERES), Barcelona, Spain.
  • Cordeiro A; Molecular Oncology and Embryology Laboratory, Human Anatomy Unit, School of Medicine, University of Barcelona, IDIBAPS, Barcelona, Spain.
  • Saco A; Department of Pathology, The Biomedical Diagnostic Center, Hospital Clinic of Barcelona, University of Barcelona, IDIBAPS (August Pi i Sunyer Biomedical Research Institute), CIBERES, Barcelona, Spain.
  • Muñoz C; Molecular Oncology and Embryology Laboratory, Human Anatomy Unit, School of Medicine, University of Barcelona, IDIBAPS, Barcelona, Spain.
  • Fuster D; Molecular Oncology and Embryology Laboratory, Human Anatomy Unit, School of Medicine, University of Barcelona, IDIBAPS, Barcelona, Spain.
  • Molins L; Department of Thoracic Surgery, Thorax Clínic Institute, Hospital Clinic of Barcelona, University of Barcelona, Barcelona, Spain.
  • Ramirez J; Department of Pathology, The Biomedical Diagnostic Center, Hospital Clinic of Barcelona, University of Barcelona, IDIBAPS (August Pi i Sunyer Biomedical Research Institute), CIBERES, Barcelona, Spain.
  • Monzo M; Molecular Oncology and Embryology Laboratory, Human Anatomy Unit, School of Medicine, University of Barcelona, IDIBAPS, Barcelona, Spain.
J Thorac Oncol ; 11(12): 2173-2182, 2016 12.
Article em En | MEDLINE | ID: mdl-27496652
ABSTRACT

INTRODUCTION:

Long intergenic noncoding RNA-p21 (lincRNA-p21) is a long noncoding RNA transcriptionally activated by tumor protein p53 (TP53) and hypoxia inducible factor 1 alpha subunit (HIF1A). It is involved in the regulation of TP53-dependent apoptosis and the Warburg effect. We have investigated the role of lincRNA-p21 in NSCLC.

METHODS:

LincRNA-p21 expression was assessed in tumor and normal tissue from 128 patients with NSCLC and correlated with time to relapse and cancer-specific survival (CSS). H23, H1299, and HCC-44 cell lines were cultured in hypoxic conditions after silencing of lincRNA-p21. The TaqMan human angiogenesis array was used to explore angiogenesis-related gene expression. Levels of the protein vascular endothelial growth factor A were measured by enzyme-linked immunosorbent assay in the cell supernatants. Angiogenic capability was measured by human umbilical vein endothelial cell tube formation assay. Microvascular density in tumor samples was analyzed by immunohistochemistry.

RESULTS:

LincRNA-p21 was down-regulated in tumor tissue, but no association was observed with TP53 mutational status. High lincRNA-p21 levels were associated with poor CSS in all patients (p = 0.032). When patients were classified according to histological subtypes, the impact of lincRNA-p21 was confined to patients with adenocarcinoma in both time to relapse (p = 0.006) and CSS (p < 0.001). To explain the poor outcome of patients with high lincRNA-p21 expression, we studied the role of lincRNA-p21 in angiogenesis in vitro and observed a global downregulation in the expression of angiogenesis-related genes when lincRNA-p21 was inhibited. Moreover, supernatants from lincRNA-p21-inhibited cells were significantly less angiogenic and had lower levels of secreted vascular endothelial growth factor A than controls did. Finally, tumor samples with high lincRNA-p21 levels had higher microvascular density.

CONCLUSIONS:

Our findings suggest that lincRNA-p21 affects outcome in patients with NSCLC adenocarcinoma through the regulation of angiogenesis.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteínas Proto-Oncogênicas p21(ras) / Carcinoma Pulmonar de Células não Pequenas / RNA Longo não Codificante / Neoplasias Pulmonares Tipo de estudo: Prognostic_studies Limite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: J Thorac Oncol Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Espanha

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteínas Proto-Oncogênicas p21(ras) / Carcinoma Pulmonar de Células não Pequenas / RNA Longo não Codificante / Neoplasias Pulmonares Tipo de estudo: Prognostic_studies Limite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: J Thorac Oncol Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Espanha